[HTML][HTML] Opportunistic genomic screening. Recommendations of the European society of human genetics

G de Wert, W Dondorp, A Clarke… - European Journal of …, 2021 - nature.com
If genome sequencing is performed in health care, in theory the opportunity arises to take a
further look at the data: opportunistic genomic screening (OGS). The European Society of …

A framework for reporting secondary and incidental findings in prenatal sequencing: When and for whom?

D Vears, DJ Amor - Prenatal diagnosis, 2022 - Wiley Online Library
As the use of genomic sequencing (GS) in the prenatal setting becomes more widespread,
laboratories and clinicians will be tasked with making decisions about whether to offer …

Introducing Edna: a trainee chatbot designed to support communication about additional (secondary) genomic findings

D Ireland, DK Bradford, E Szepe, E Lynch… - Patient education and …, 2021 - Elsevier
Objective To support informed decision-making about reanalysis of clinical genomic data for
risk of preventable conditions ('additional findings') by developing a chatbot (electronic …

[HTML][HTML] Evaluation of a two-step model of opportunistic genomic screening

M Martyn, L Lee, A Jan, E Lynch… - European Journal of …, 2024 - nature.com
Increasing use of diagnostic genomic sequencing is pushing health services to confront the
issue of opportunistic genomic screening (OGS). To date, OGS has been offered …

Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol

SE Bouffler, L Lee, F Lynch, M Martyn, E Lynch… - BMJ open, 2023 - bmjopen.bmj.com
Introduction As routine genomic testing expands, so too does the opportunity to look for
additional health information unrelated to the original reason for testing, termed additional …

[HTML][HTML] Preferences for return of germline genome sequencing results for cancer patients and their genetic relatives in a research setting

MC Best, P Butow, J Savard, C Jacobs… - European Journal of …, 2022 - nature.com
Germline genome sequencing (GS) holds great promise for cancer prevention by identifying
cancer risk and guiding prevention strategies, however research evidence is mixed …

[HTML][HTML] Eliciting parental preferences and values for the return of additional findings from genomic sequencing

I Goranitis, Y Meng, M Martyn, S Best, S Bouffler… - NPJ Genomic …, 2024 - nature.com
Health economic evidence is needed to inform the design of high-value and cost-effective
processes for returning genomic results from analyses for additional findings (AF). This study …

My Research Results: a program to facilitate return of clinically actionable genomic research findings

AM Willis, B Terrill, A Pearce, A McEwen… - European Journal of …, 2022 - nature.com
Researchers and research participants increasingly support returning clinically actionable
genetic research findings to participants, but researchers may lack the skills and resources …

[HTML][HTML] Evaluating the resource implications of different service delivery models for offering additional genomic findings

M Vu, K Degeling, M Martyn, E Lynch, B Chong… - Genetics in …, 2021 - Elsevier
Purpose To evaluate the resource implications of different delivery models for the provision
of additional findings (AF) in genomics from a health-care purchaser perspective. Methods …

[HTML][HTML] Making community voices heard in a research–health service alliance, the evolving role of the Community Advisory Group: a case study from the members' …

JL Wale, L Di Pietro, H Renton, M Sahhar… - Research Involvement …, 2021 - Springer
Abstract Background The Melbourne Genomics Health Alliance (the Alliance) is a
collaboration of leading hospitals, research and academic organisations, supported by its …